Xw. Cheng et al., POLYHEDRIN SEQUENCE DETERMINES THE TETRAHEDRAL SHAPE OF OCCLUSION BODIES IN THYSANOPLUSIA-ORICHALCEA SINGLE-NUCLEOCAPSID NUCLEOPOLYHEDROVIRUS, Journal of General Virology, 79, 1998, pp. 2549-2556
A nucleopolyhedrovirus (NPV) isolated from the looper Thysanoplusia or
ichalcea L. (Lepidoptera: Noctuidae) (ThorNPV) is occluded in a tetrah
edral protein matrix. The ORF of the ThorNPV polyhedrin gene contains
738 nt which code for 246 amino acids of the putative polyhedrin prote
in with an estimated molecular mass of 28778 Da. The promoter of this
gene is similar in length to the promoter of Spodoptera frugiperda NPV
(SfMNPV), with a 5 nt deletion before the start codon compared to tho
se of other NPVs, When the polyhedrin gene of Autographa californica N
PV (AcMNPV), whose occlusion bodies (OBs) are polyhedral, was replaced
by the polyhedrin gene of ThorNPV, which produces tetrahedral OBs, te
trahedral polyhedra with properly occluded virions were produced. This
work establishes the importance of the polyhedrin protein sequence in
determining OB shape. Leucine at position 43 of ThorNPV polyhedrin wa
s identified as responsible for the tetrahedral shape of ThorNPV OBs b
y PCR-based site-directed mutagenesis, Susceptibility to alkaline buff
er of OBs formed by recombinant AcMNPV (RECAcV) carrying the polyhedri
n gene of ThorNPV was slightly greater than that of native ThorNPV OBs
. The LD,, of RECAcV for third-instar beet armyworm (Spodoptera exigua
) was significantly lower than that of AcMNPV (253 and 31 OBs per larv
a, respectively).